autosomal dominant distal hereditary motor neuronopathy 6 Disease Ontology Browser

Home
Genes
Phenotypes
Human Disease
Expression
Recombinases
Function
Strains / SNPs
Homology
Tumors

About Help FAQ

Search
Download
More Resources
Submit Data
Find Mice (IMSR)
Analysis Tools
Contact Us
Browsers

Disease Ontology Browser

autosomal dominant distal hereditary motor neuronopathy 6 (DOID:0111210)
Alliance: disease page
Synonyms: distal hereditary motor neuronopathy type 2D; distal hereditary motor neuropathy type IID; distal spinal muscular atrophy with calf predominance; HMN2D; HMN IID
Alt IDs: OMIM:615575
Definition: A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the FBXO38 gene on 5q32.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/10/2024 MGI 6.24